Allele Registry

Canonical Allele Identifier: PA115057

Gene: HPD HGNC NCBI

ClinVar RCV:

RCV000001639

RCV001297386

RCV001731268

ClinVar Variation:

1573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165464.1:p.Tyr121Cys	CA115056 NM_001171993.2:c.362A>G